ENST00000373247.7:c.1745A>C
MANE Select
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ENSP00000362344.2:p.Glu582Ala
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ENST00000373225.7:c.1595A>C
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ENSP00000362322.3:p.Glu532Ala
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ENST00000373247.6:c.1745A>C
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ENSP00000362344.2:p.Glu582Ala
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ENST00000393706.6:c.1667A>C
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ENSP00000377309.2:p.Glu556Ala
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ENST00000460181.5:n.1733A>C
|
|
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ENST00000467826.5:n.709+262A>C
|
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ENST00000630236.2:c.*469A>C
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ENSP00000486766.1:n.*469A>C
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NM_001018078.2:c.1595A>C
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NP_001018088.1:p.Glu532Ala
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|
NM_001288803.1:c.1667A>C
|
NP_001275732.1:p.Glu556Ala
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NM_004957.5:c.1745A>C
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NP_004948.4:p.Glu582Ala
|
|
NR_110170.1:n.1793A>C
|
|
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XM_005251864.2:c.1483+262A>C
|
XP_005251921.1:n.1483+262A>C
|
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XM_011518437.1:c.1595A>C
|
XP_011516739.1:p.Glu532Ala
|
|
XM_011518438.1:c.1595A>C
|
XP_011516740.1:p.Glu532Ala
|
|
XM_011518439.1:c.902A>C
|
XP_011516741.1:p.Glu301Ala
|
|
XR_242581.2:n.1642A>C
|
|
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XR_242582.2:n.1380+262A>C
|
|
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XM_005251864.4:c.1483+262A>C
|
XP_005251921.1:n.1483+262A>C
|
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XM_011518439.2:c.902A>C
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XP_011516741.1:p.Glu301Ala
|
|
XM_017014565.2:c.1333+262A>C
|
XP_016870054.1:n.1333+262A>C
|
|
XM_017014566.1:c.902A>C
|
XP_016870055.1:p.Glu301Ala
|
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XR_242581.4:n.1640A>C
|
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XR_242582.4:n.1378+262A>C
|
|
|
NM_004957.6:c.1745A>C
MANE Select
|
NP_004948.4:p.Glu582Ala
|
|